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Reena Das

Showing results (231-240 of 280) with videos related to

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Computers in Biology and Medicine|April 27, 2025
Detection of β-Thalassemia trait from a heterogeneous population with red cell indices and parametersSubrata Saha, Prashant Sharma, Atul Kumar Jain, et al.
Croatian Medical Journal|June 13, 2024
Non-invasive prenatal testing of beta-hemoglobinopathies using next generation sequencing, in-silico sequence size selection, and haplotypingHenry A Erlich, Lily Ko, Jiyae Lee, et al.
Tropical Medicine & International Health : TM & IH|January 8, 2021
Evaluation of a flow cytometric test for G6PD-deficient erythrocytesAlpeshkumar Bipinbhai Kapadia, Prashant Sharma, Karuna Jain, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|December 26, 2022
Molecular spectrum of inherited FVII deficiency in North India revealed a recurrent variant with a founder effectRitika Sharma, Manu Jamwal, Hari Kishan Senee, et al.
Bio-Protocol|October 13, 2025
Standardized Culture of Skin Fibroblasts From Punch Biopsies for Germline DNA Isolation in Myeloid Malignancies: A Practical Bedside-to-Laboratory ApproachParampreet Kour, Nedhi Kumari, Naveen Kaushal, et al.
The Journal of Applied Laboratory Medicine|December 1, 2021
Noninvasive Prenatal Test for β-Thalassemia and Sickle Cell Disease Using Probe Capture Enrichment and Next-Generation Sequencing of DNA in Maternal PlasmaHenry A Erlich, Christian López-Peña, Katie T Carlberg, et al.
Hematology (Amsterdam, Netherlands)|March 12, 2015
Role of blood and bone marrow examination in the diagnosis of mature lymphoid neoplasms in patients presenting with isolated splenomegalySreejesh Sreedharanunni, Man Updesh Singh Sachdeva, Pankaj Malhotra, et al.
Leukemia Research|December 2, 2021
Chronic eosinophilic leukemia with recurrent STAT5B N642H mutation-An entity with features of myelodysplastic syndrome/ myeloproliferative neoplasm overlapSreejesh Sreedharanunni, Manu Jamwal, Anand Balakrishnan, et al.
Annals of Hematology|July 18, 2020
A high frequency of Gilbert syndrome (UGT1A1*28/*28) and associated hyperbilirubinemia but not cholelithiasis in adolescent and adult north Indian patients with transfusion-dependent β-thalassemiaOshan Shrestha, Alka Rani Khadwal, Manphool Singhal, et al.
Retina (Philadelphia, Pa.)|October 10, 2014
Thrombophilic risk factors are uncommon in young patients with retinal vein occlusionJasmina Ahluwalia, Sandeep Rao, Subhash Varma, et al.
Pageof 28

Showing results (231-240 of 280) with videos related to

Sort By:
Pageof 28
Computers in Biology and Medicine|April 27, 2025
Detection of β-Thalassemia trait from a heterogeneous population with red cell indices and parametersSubrata Saha, Prashant Sharma, Atul Kumar Jain, et al.
Croatian Medical Journal|June 13, 2024
Non-invasive prenatal testing of beta-hemoglobinopathies using next generation sequencing, in-silico sequence size selection, and haplotypingHenry A Erlich, Lily Ko, Jiyae Lee, et al.
Tropical Medicine & International Health : TM & IH|January 8, 2021
Evaluation of a flow cytometric test for G6PD-deficient erythrocytesAlpeshkumar Bipinbhai Kapadia, Prashant Sharma, Karuna Jain, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|December 26, 2022
Molecular spectrum of inherited FVII deficiency in North India revealed a recurrent variant with a founder effectRitika Sharma, Manu Jamwal, Hari Kishan Senee, et al.
Bio-Protocol|October 13, 2025
Standardized Culture of Skin Fibroblasts From Punch Biopsies for Germline DNA Isolation in Myeloid Malignancies: A Practical Bedside-to-Laboratory ApproachParampreet Kour, Nedhi Kumari, Naveen Kaushal, et al.
The Journal of Applied Laboratory Medicine|December 1, 2021
Noninvasive Prenatal Test for β-Thalassemia and Sickle Cell Disease Using Probe Capture Enrichment and Next-Generation Sequencing of DNA in Maternal PlasmaHenry A Erlich, Christian López-Peña, Katie T Carlberg, et al.
Hematology (Amsterdam, Netherlands)|March 12, 2015
Role of blood and bone marrow examination in the diagnosis of mature lymphoid neoplasms in patients presenting with isolated splenomegalySreejesh Sreedharanunni, Man Updesh Singh Sachdeva, Pankaj Malhotra, et al.
Leukemia Research|December 2, 2021
Chronic eosinophilic leukemia with recurrent STAT5B N642H mutation-An entity with features of myelodysplastic syndrome/ myeloproliferative neoplasm overlapSreejesh Sreedharanunni, Manu Jamwal, Anand Balakrishnan, et al.
Annals of Hematology|July 18, 2020
A high frequency of Gilbert syndrome (UGT1A1*28/*28) and associated hyperbilirubinemia but not cholelithiasis in adolescent and adult north Indian patients with transfusion-dependent β-thalassemiaOshan Shrestha, Alka Rani Khadwal, Manphool Singhal, et al.
Retina (Philadelphia, Pa.)|October 10, 2014
Thrombophilic risk factors are uncommon in young patients with retinal vein occlusionJasmina Ahluwalia, Sandeep Rao, Subhash Varma, et al.
Pageof 28